BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 9630071)

  • 1. DNA diagnosis of FRAXA and FRAXE in Chinese children with neurodevelopmental disorders and fragile X syndrome.
    Chan SY; Wong V
    Clin Genet; 1998 Mar; 53(3):179-83. PubMed ID: 9630071
    [TBL] [Abstract][Full Text] [Related]  

  • 2. FRAXA and FRAXE: the results of a five year survey.
    Youings SA; Murray A; Dennis N; Ennis S; Lewis C; McKechnie N; Pound M; Sharrock A; Jacobs P
    J Med Genet; 2000 Jun; 37(6):415-21. PubMed ID: 10851251
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers.
    Murray A; Youings S; Dennis N; Latsky L; Linehan P; McKechnie N; Macpherson J; Pound M; Jacobs P
    Hum Mol Genet; 1996 Jun; 5(6):727-35. PubMed ID: 8776586
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The influence of expanded unmethylated alleles for FRAXA/FRAXE loci in the intellectual performance among Brazilian mentally impaired males.
    Barros Santos C; Gonçalves Pimentel MM
    Int J Mol Med; 2003 Sep; 12(3):385-9. PubMed ID: 12883656
    [TBL] [Abstract][Full Text] [Related]  

  • 5. FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population.
    Syrrou M; Georgiou I; Grigoriadou M; Petersen MB; Kitsiou S; Pagoulatos G; Patsalis PC
    Genet Epidemiol; 1998; 15(1):103-9. PubMed ID: 9523214
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A survey of FRAXE allele sizes in three populations.
    Zhong N; Ju W; Curley D; Wang D; Pietrofesa J; Wu G; Shen Y; Pang C; Poon P; Liu X; Gou S; Kajanoja E; Ryynänen M; Dobkin C; Brown WT
    Am J Med Genet; 1996 Aug; 64(2):415-9. PubMed ID: 8844095
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission.
    Murray A; Macpherson JN; Pound MC; Sharrock A; Youings SA; Dennis NR; McKechnie N; Linehan P; Morton NE; Jacobs PA
    Hum Mol Genet; 1997 Feb; 6(2):173-84. PubMed ID: 9063737
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.
    Patsalis PC; Sismani C; Hettinger JA; Boumba I; Georgiou I; Stylianidou G; Anastasiadou V; Koukoulli R; Pagoulatos G; Syrrou M
    Am J Med Genet; 1999 May; 84(3):184-90. PubMed ID: 10331587
    [TBL] [Abstract][Full Text] [Related]  

  • 9. FRAXE expansion is not a common etiological factor among developmentally delayed males.
    Allingham-Hawkins DJ; Ray PN
    Am J Hum Genet; 1995 Jul; 57(1):72-6. PubMed ID: 7541938
    [TBL] [Abstract][Full Text] [Related]  

  • 10. FRAXE mutation in mentally retarded patients using the OxE18 probe.
    Mulatinho MV; Llerena JC; Pimentel MM
    Int J Mol Med; 2000 Jan; 5(1):67-9. PubMed ID: 10601577
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males.
    Biancalana V; Taine L; Bouix JC; Finck S; Chauvin A; De Verneuil H; Knight SJ; Stoll C; Lacombe D; Mandel JL
    Am J Hum Genet; 1996 Oct; 59(4):847-54. PubMed ID: 8808600
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new PCR assay useful for screening of FRAXE/FMR2 mental impairment among males.
    Santos CB; Costa Lima MA; Pimentel MM
    Hum Mutat; 2001 Aug; 18(2):157-62. PubMed ID: 11462240
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom.
    Knight SJ; Ritchie RJ; Chakrabarti L; Cross G; Taylor GR; Mueller RF; Hurst J; Paterson J; Yates JR; Dow DJ; Davies KE
    Am J Hum Genet; 1996 May; 58(5):906-13. PubMed ID: 8651274
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles.
    Brown TC; Tarleton JC; Go RC; Longshore JW; Descartes M
    Am J Med Genet; 1997 Dec; 73(4):447-55. PubMed ID: 9415473
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular screening of FRAXA and FRAXE in Indian patients with unexplained mental retardation.
    Pandey UB; Phadke S; Mittal B
    Genet Test; 2002; 6(4):335-9. PubMed ID: 12537661
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation.
    Farzin F; Perry H; Hessl D; Loesch D; Cohen J; Bacalman S; Gane L; Tassone F; Hagerman P; Hagerman R
    J Dev Behav Pediatr; 2006 Apr; 27(2 Suppl):S137-44. PubMed ID: 16685180
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Simultaneous Screening of the FRAXA and FRAXE Loci for Rapid Detection of FMR1 CGG and/or AFF2 CCG Repeat Expansions by Triplet-Primed PCR.
    Liu T; Wang FS; Cheah FSH; Gu Y; Shaw M; Law HY; Tay SKH; Lee CG; Nelson DL; Gecz J; Chong SS
    J Mol Diagn; 2021 Aug; 23(8):941-951. PubMed ID: 34111553
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation.
    Major T; Culjkovic B; Stojkovic O; Gucscekic M; Lakic A; Romac S
    J Neurogenet; 2003; 17(2-3):223-30. PubMed ID: 14668200
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India.
    Guruju MR; Lavanya K; Thelma BK; Sujatha M; OmSai VR; Nagarathna V; Amarjyothi P; Jyothi A; Anandaraj MP
    J Clin Neurosci; 2009 Oct; 16(10):1305-10. PubMed ID: 19560928
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cognitive, behavioral, and neuroanatomical assessment of two unrelated male children expressing FRAXE.
    Abrams MT; Doheny KF; Mazzocco MM; Knight SJ; Baumgardner TL; Freund LS; Davies KE; Reiss AL
    Am J Med Genet; 1997 Feb; 74(1):73-81. PubMed ID: 9034011
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.